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  • 1
    In: European Journal of Heart Failure, Wiley, Vol. 21, No. 4 ( 2019-04), p. 462-470
    Abstract: Klotho, an essential co‐receptor for fibroblast growth factor (FGF)‐23, has potentially beneficial inhibitory effects on the renin–angiotensin system. Limited data exist on the prognostic value of Klotho and FGF‐23 levels in combination or their ability to predict benefit from angiotensin‐converting enzyme (ACE) inhibition. Methods and results A total of 3555 patients with stable ischaemic heart disease and left ventricular ejection fraction 〉  40% enrolled in the PEACE trial of trandolapril vs. placebo had Klotho levels drawn at randomization. Patients were characterized by quartiles of Klotho and FGF‐23 concentrations. Six‐year Kaplan–Meier rates and adjusted risk were calculated in the placebo arm for the composite of cardiovascular (CV) death or hospitalization for heart failure and its components. Low [quartile (Q) 1–3] Klotho concentration was associated with an increased rate of CV death or hospitalization for heart failure as compared with Q4 (8.2% vs. 4.2%; P  = 0.03). After multivariable adjustment for clinical variables and renal and CV biomarkers (estimated glomerular filtration rate, cystatin‐C, urine albumin‐to‐creatinine ratio, FGF‐23, high‐sensitivity troponin T, N‐terminal pro‐B‐type natriuretic peptide, and high‐sensitivity C‐reactive protein), low Klotho concentration remained strongly associated with increased risk of CV death or hospitalization for heart failure [adjusted hazard ratio (HR) 2.62; 95% confidence interval (CI) 1.35–5.08; P   〈  0.01]. The combination of low Klotho and high (Q4) FGF‐23 concentration identified patients at particularly elevated risk (adjusted HR 3.99; 95% CI 1.67–9.56; P   〈  0.01). This high‐risk combination additionally predicted benefit from trandolapril (HR 0.39; 95% CI 0.23–0.68; P interaction   〈  0.01). Conclusions Low Klotho concentration is associated with an increased risk of CV death or heart failure hospitalization in patients with stable ischaemic heart disease. The combination of low Klotho and high FGF‐23 further identifies patients at distinctly elevated risk who derive clinical benefit from the ACE‐inhibitor trandolapril.
    Type of Medium: Online Resource
    ISSN: 1388-9842 , 1879-0844
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 1500332-2
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  • 2
    In: Clinical Cardiology, Wiley, Vol. 45, No. 7 ( 2022-07), p. 794-801
    Abstract: Trial Evaluating Cardiovascular Outcomes with Sitagliptin (TECOS) assessed the cardiovascular (CV) safety of sitagliptin versus placebo on CV outcomes in patients with type 2 diabetes and CV disease and found sitagliptin noninferior to placebo. Subsequently, based on feedback from FDA, the Sponsor of the trial, Merck & Co., Inc., engaged a separate academic research organization, the TIMI Study Group, to re‐adjudicate a prespecified set of originally adjudicated events. Methods TIMI adjudicated in a blinded fashion all potential hospitalization for heart failure (HHF) events, all potential MACE+ events previously adjudicated as not an endpoint event, and a random subset (~10%) of MACE+ events previously adjudicated as an endpoint event. An updated study‐level meta‐analysis of four randomized, placebo‐controlled, CV outcomes trials with dipeptidyl peptidase 4 (DPP‐4) inhibitors was then performed. Results After re‐adjudication of potential HHF events in the intent‐to‐treat population, there were 224 patients with a confirmed event in the sitagliptin arm (1.05/100 person‐years) and 239 patients in the placebo arm (1.13/100 person‐years), corresponding to a hazard ratio (HR) of 0.94 (95% confidence interval [95% CI]: 0.78–1.13, p  = .49). Concordance between the outcome of the original adjudication and the re‐adjudication for HHF events was 82.7%. The meta‐analysis of CV outcomes trials with DPP‐4 inhibitors with placebo and involving 43 522 patients yielded an HR of 1.07 (95% CI: 0.83–1.39), with moderate heterogeneity ( p  = .45, I 2  = 62.07%). Conclusion The results of this independent re‐adjudication process and analyses of CV outcomes from TECOS were consistent with the original adjudication results and overall study findings. An updated study‐level meta‐analysis showed no overall significant risk for HHF with DPP‐4 inhibitors, but with statistical heterogeneity.
    Type of Medium: Online Resource
    ISSN: 0160-9289 , 1932-8737
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 2048223-1
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